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Electroacupuncture for Amnestic Mild Cognitive Impairment: A Randomized Controlled Trial

Clinical Study on Electroacupuncture for Amnestic Mild Cognitive Impairment

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026000417
Enrollment
Unknown
Registered
2026-02-25
Start date
2026-04-01
Completion date
Unknown
Last updated
2026-03-02

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Mild Cognitive Impairment

Interventions

Electroacupuncture Group:After routine skin disinfection of the acupoints Baihui (GV20), Sishencong (EX-HN1), Shenting (GV24), Yintang (EX-HN3), Fengchi (GB20, bilateral), Yingxiang (LI20, bilateral),
Sham Electroacupuncture Group:The subject assumed a supine position. Non-meridian, non-acupoint locations on the arms and legs were selected as sham points: Sham Point 1: 8 cm proximal to the cubita

Sponsors

the First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
50 Years to 85 Years

Inclusion criteria

Inclusion criteria: Diagnostic Criteria: Based on the Western diagnostic criteria proposed by Jak/Bondi in 2014, the following six indicators were used: Delayed free recall (N5) and recognition (N7) scores from the Auditory Verbal Learning Test Huashan version (AVLT) Total score of the Animal Fluency Test (AFT) Total score of the Boston Naming Test (BNT) Total completion time of Shape Trails Test-A and B (STT-A/B) Diagnosis is confirmed if: 1) Two test scores within the same cognitive domain are impaired; 2) Or one test score in each of the three cognitive domains (memory, executive function, language) is impaired; 3) Or activities of daily living are impaired. Among these, aMCI is diagnosed based on the MCI diagnostic criteria, with impairment in AVLT N5 and/or AVLT N7. Inclusion Criteria: (1) Meet the diagnostic criteria for aMCI; (2) Aged between 50 and 85 years (inclusive), regardless of gender; (3) Disease duration exceeding 3 months; (4) Clinical Dementia Rating (CDR) score of 0.5; (5) Ischemic Index score < 4; (6) Ability to comprehend and complete assessments correctly; (7) Voluntary participation and signed informed consent; (8) No contraindications to MRI scanning (e.g., metal implants).

Exclusion criteria

Exclusion criteria: (1) Currently undergoing treatments that may interfere with cognitive function; (2) A history of neurological disorders affecting cognition or systemic diseases leading to cognitive decline, except for individuals with suspected early-stage Alzheimer's disease; (3) Brain magnetic resonance imaging (MRI) findings indicating infections, other focal lesions, multiple infarctions, infarcts in critical memory-related brain regions, or severe white matter lesions; (4) A history of tumors, psychiatric disorders, or severe anxiety and depression; (5) Presence of hemorrhagic diseases, bleeding tendencies, or severe skin infections; (6) Severe drug dependence, smoking, substance abuse, or alcohol addiction; (7) Pregnant or lactating individuals, or those with suspected pregnancy; (8) Having received any acupuncture treatment or participated in other clinical trials within the past six months; (9) Individuals with skin breakdown, infections, or susceptibility to allergies at acupuncture points, or those with claustrophobia.

Design outcomes

Primary

MeasureTime frame
Montreal Cognitive Assessment Scale;

Secondary

MeasureTime frame
Alzheimer's Disease Assessment Scale-Cognitive Subscale; Pittsburgh Sleep Quality Index;Traditional Chinese Medicine (TCM) Syndrome Score Scale;

Countries

China

Contacts

Public ContactQuan Fei

The First Affiliated Hospital of Guizhou University of Traditional Chinese Medicine

2417891021@qq.com+86 15585107127

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Mar 14, 2026